Motor Neurone Disease, fighting it together.

Hello, my name is Lesley Roberts and my husband Christopher, who was a farmer, was diagnosed with MND on May 5th 2014, sadly he lost his courageous fight with this awful disease on September 5th 2015. I wrote this blog to share our journey as a family with this disease, the good days and the bad days and hope to raise awareness of MND in the process.

Saturday, 28 June 2014

No.11.Time to smile

Today is our youngest daughter`s 19th birthday. It isn`t time to dwell on regrets for the future, but to celebrate today and bloody well have some fun. You ain`t taking this away from us MND.!
Posted by soulpixie at 06:52
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Blog Archive

  • ▼  2014 (141)
    • ▼  June (14)
      • No.1.Confirmation = devastation
      • No.2.Facing reality
      • No.3.Life goes on.
      • No.4.Trying to stay positive.
      • No.5.Privacy and normality.
      • No.6.The voice expresses our soul .
      • No.7.Being normal
      • No.8.Kindness in it`s many ways
      • No.9.Manifestations of festiculations
      • No.10.Time to adjust, time to think
      • No.11.Time to smile
      • No.12.Memories made.
      • No.13.Stolen futures.
      • No.14.Virtual hugs.
    • ►  July (30)
    • ►  August (31)
    • ►  September (23)
    • ►  October (24)
    • ►  November (10)
    • ►  December (9)
  • ►  2015 (129)
    • ►  January (11)
    • ►  February (12)
    • ►  March (8)
    • ►  April (8)
    • ►  May (17)
    • ►  June (13)
    • ►  July (19)
    • ►  August (23)
    • ►  September (8)
    • ►  October (3)
    • ►  November (2)
    • ►  December (5)
  • ►  2016 (12)
    • ►  January (5)
    • ►  February (5)
    • ►  March (2)

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